A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210921



Internal ID22358652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30684087..30684187hg38UCSC Ensembl
chr13:31258224..31258324hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14367988, nssv14367985, nssv14367987, nssv14367986, nssv14367989
SamplesNA19239, HG00731, NA19240, HG00733, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210921
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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